Biopharma Transcript

Clearmind Medicine Inc. CMND

Nasdaq · Phase 1 · CNS/neurology/psychiatry · small molecule · EDGAR · Updated Nov 4, 2026

Clearmind Medicine Inc. (Nasdaq: CMND) is a CNS/neurology/psychiatry drug developer. Its lead program, Psychedelic-derived candidates (e.g. MEAI-based), is in Phase 1 for Alcohol use disorder and other CNS indications.

Upcoming catalysts

No catalyst is dated to the next 30 days or to an FDA action date.

Pipeline

ProgramIndicationModalityStage
Lead psychedelic programsAUDsmall moleculePhase 1

Recent results and decisions

  1. Sep 8, 2026
    met Part A: all 24 participants across four ascending-dose cohorts completed treatment; primary safety and tolerability endpoint achieved, no SAEs (recap of prior announcement).The study achieved its primary endpoint of safety and tolerability. Filing
  2. Apr 14, 2026
    met Met primary safety and tolerability endpoint in dose-escalation; no serious adverse events in cohort 3 at higher dose.Meeting the primary safety and tolerability endpoint in this dose-escalation stage, including at the higher dosage in the third cohort, supports continued advancement of CMND-100 as a potential novel, non-hallucinogenic treatment option for AUD. Filing
  3. Feb 9, 2026
    positive Cohort 2 topline safety: no serious adverse events and overall good tolerability.The results reinforce no serious adverse events and overall good tolerability, consistent with the favorable results reported from the first cohort Filing

2 more on record.

For subscribers

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